Colon Cancer: Gene >> DNM1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000549701
Start	32740221:32740221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1865C>T
AA Mutation	p.Ala622Val(p.A622V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000549701
Start	32738278:32738278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1689C>G
AA Mutation	p.Ser563Arg(p.S563R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000549701
Start	32731061:32731061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1127G>A
AA Mutation	p.Arg376Gln(p.R376Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000549701
Start	32740440:32740440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1916G>A
AA Mutation	p.Arg639Gln(p.R639Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000549701
Start	32707400:32707400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.284A>G
AA Mutation	p.His95Arg(p.H95R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000549701
Start	32740127:32740127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1771G>T
AA Mutation	p.Gly591Ter(p.G591*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000549701
Start	32708183:32708183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328G>T
AA Mutation	p.Glu110Ter(p.E110*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000549701
Start	32738285:32738285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1696G>T
AA Mutation	p.Glu566Ter(p.E566*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DNM1L

No Mutation Annotation!